rs387906822, OSMR

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1
5 0.925 0.120 5 38925240 missense variant C/T snv 3.2E-05 0.800 1.000 2 2008 2010
Familial lichen amyloidosis
CUI: C0268398
Disease: Familial lichen amyloidosis
24 0.925 0.120 5 38925240 missense variant C/T snv 3.2E-05 0.010 1.000 1 2010 2010